Design of enediyne prodrugs.
M. E. Maier, Synlett, 1995, 13.
Key Words:
GENERAL STRATEGIES FOR GENERATING REACTIVE ENEDIYNES/FACTORS THAT INFLUENCE
THE REACTIVITY OF ENEDIYNES/1,5-DIYNES AS PRODRUGS/ENEDIYNE PRODRUGS WITH A
BRIDGEHEAD DOUBLE BOND/ENEDIYNE PRODRUGS WITH AN EPOXIDE AS BLOCKING DEVICE/OTHER
ENEDIYNE-CONTAINING PRODRUGS/CONCLUSION/CALICHEAMICIN-ESPERAMICIN ANALOGS/CYCLIC
CONJUGATED ENEDIYNES/DNA-CLEAVING MOLECULES/DYNEMICIN-A/ANTITUMOR ANTIBIOTICS/CHEMICAL
SYNTHESIS/DYOTROPIC REARRANGEMENTS/ANTICANCER ANTIBIOTICS/BIRADICAL FORMATION/TRIGGERING
DEVICES
Synthesis of medium-sized rings by the ring-closing metathesis reaction.
M. E. Maier, Angew. Chem., Int. Ed. Engl., 2000, 39, 2073.
Key Words:
cyclizations/medium-sized rings/metathesis/synthetic methods/OLEFIN
METATHESIS/EPOTHILONE-A/IMIDAZOLIN-2-YLIDENE LIGANDS/NORTHERN-HEMISPHERE/ORGANIC-SYNTHESIS/BICYCLIC
LACTAMS/10-MEMBERED RING/ROSEOPHILIN/CONSTRUCTION/COMPLEXES
Design and synthesis of dynemicin analogs.
M. E. Maier, F. Bosse, A. J. Niestroj, Eur. J. Org. Chem., 1999,
1.
Key Words:
dynemicin/enediynes/antitumor agents/antibiotics/cross-coupling/ANTITUMOR
ANTIBIOTIC DYNEMICIN/WIDE STRUCTURAL VARIABILITY/ARYL CARBAMATE MOIETIES/CHEMICAL
SYNTHESIS/MOLECULAR DESIGN/DNA-CLEAVAGE/CYCLIC ENEDIYNES/BIOLOGICAL PROPERTIES/BIOACTIVE
ANALOGS/METHIDE FORMATION